Canonical Allele Identifier: PA2825577093
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met1592Arg
CA394308151
NM_001114382.3:c.4775T>G